FDA Inspection 822054 — Northwest Medical Center Irb
The FDA completed an inspection of Northwest Medical Center Irb on Feb 15, 2013 in Tucson, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Feb 15, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Tucson, AZ (United States)
Additional Details
IRB